Linawati Sutrisno
;
Kewei Sun
;
Katsuhiko Ariga
説明:
(abstract)Visualization of RNA and DNA provides a window of opportunity for earlier detection of multiple diseases and approach to manipulate it before any pathological processes occur. Yet, current imaging systems often fail to meet these demands due to need of multiple RNA and DNA chemical probes, which increases experimental complexity, reduces awareness of false positives, and limits imaging accuracy in complex biosystems. In this progress, we identify the key challenges associated with using multiple probes for RNA and DNA imaging and analyze the mechanisms and performance of existing imaging tools. This article also introduces a conceptual framework and proposes a multidisciplinary framework to guide the next generation of imaging technologies. Furthermore, we highlight how nanoarchitectonics-based molecular design can enable single-step, multiplexed RNA–DNA imaging. Our goal is to provide valuable resource for both biologists and probe developers for choosing the suitable molecular probes and further advance their design, from initial concepts to commercial products—all from a biologist’s perspective.
権利情報:
キーワード: RNA, DNA, bioimaging, chemical probes, multiplex, in vitro, biologist, chemist, detection
刊行年月日: 2026-03-03
出版者: American Chemical Society (ACS)
掲載誌:
研究助成金:
原稿種別: 出版者版 (Version of record)
MDR DOI:
公開URL: https://doi.org/10.1021/acsnano.5c22282
関連資料:
その他の識別子:
連絡先:
更新時刻: 2026-03-04 13:01:23 +0900
MDRでの公開時刻: 2026-03-04 18:12:11 +0900
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ACSNano26_20_6493.pdf
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サイズ | 4.98MB | 詳細 |